Реакция #1543044
ord-e533b185bc754ec9b41126b30609ce18
Уравнение реакции
Реактанты
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Условия реакции
Обработка
- 1Фильтрацияsuction filtered
- 2workup.ADDITIONThe filtrate was diluted with 400 mL of water
- 3Экстракцияextracted with four 50 mL portions of methylene chloride
- 4СушкаThe combined extracts were dried with magnesium sulfate
- 5Другоеthe solvent was removed by rotary evaporation
Методика
This example illustrates the preparation of Compound 80, namely, dimethyl 2-(cyanomethoxy)-4-(2-methylpropyl)-6-(trifluoromethyl)-3, 5-pyridine-dicarboxylate. A solution of 6.38 g (0.019 mol) of dimethyl 2-hydroxy-4-(2-methylpropyl)-6-(trifluoromethyl)- 3, 5-pyridinedicarboxylate (Compound 1) in 50 mL of dimethylformamide was prepared and to it was added 7.2 g (0.06 mol) of bromoacetonitrile and 8.3 g (0.06 mol) of anhydrous potassium carbonate. The mixture was stirred at room temperature overnight then suction filtered. The filtrate was diluted with 400 mL of water and extracted with four 50 mL portions of methylene chloride. The combined extracts were dried with magnesium sulfate and the solvent was removed by rotary evaporation giving 7.09 g (98.9% yield) of a dark amber oil. Silica gel chromatography with 10% ethyl acetate, 90% cyclohexane gave 3.51 g (49%) of Compound 80 as a clear colorless oil.